Staff Oncology Data Product Manager

npowermedicine; Redwood City (CA); Sur place; USD 168 000 - 215 000; Plein temps

Avantages offerts par ce poste

Equity at hire

Discretionary annual bonus

401K plan

Résumé du poste

N-Power Medicine is seeking a Senior Product Manager to own the oncology data platform, aligning data strategy with ProECA studies and regulatory requirements. You will drive the roadmap, define customers, and deliver regulated, high-quality data solutions for clinical trials.

You will work with engineers, biostatisticians, oncologists, and abstracts to ensure traceable, compliant data flows and actionable insights, while communicating clearly with sponsors and health systems.

Qualifications

• 8+ years of product management experience owning a healthcare data product in a regulated environment.
• Deep background in oncology clinical data: AJCC staging, histology, biomarker and genomic testing, lines of therapy, RECIST endpoints.
• Working command of FDA guidance on externally controlled trials, use of EHR data in clinical investigations, 21 CFR Part 11, ICH GCP, CDISC (SDTM, ADaM), and HIPAA.
• Deep knowledge of EHR data structures and workflows (HL7, FHIR), clinical terminologies (ICD-10, SNOMED CT, LOINC, RxNorm, NCI Thesaurus).
• Strong grounding in data platform architecture, data modeling, normalization, and transformation.
• Experience writing functional and technical specifications for data platforms.
• Strong analytical skills and data intuition: uses metrics to evaluate decisions and drive action.
• Exceptional written and verbal communication, with a track record of aligning oncologists, abstractors, biostatisticians, and engineers.

Responsabilités

• Own the vision, strategy, roadmap and requirements for the oncology data platform, aligned with business goals and ProECA studies.
• Manage the platform as a product: define customers, set success metrics, and track adoption and value.
• Collaborate with a cross-functional team of engineers, data architects, informaticists, AI engineers, and clinical staff.
• Build regulatory-grade evidence into the platform: traceability, provenance, audit trails and data quality per FDA guidelines.
• Catalog end-user documentation: data dictionaries, vocabularies, CDISC specs, data quality scorecards, licensing, de-identification.

Connaissances

Healthcare data product

Oncology clinical data

FDA guidance

HL7 FHIR

Data governance

Stakeholder communication

Agile (JIRA)

Outils

Databricks

Snowflake

APIs

JIRA

Description du poste

About N-Power Medicine

N-Power Medicine aims to establish a new paradigm in drug development by reinventing the 'how' and transforming clinical trials through better integration with clinical practice, ensuring broader participation by physicians and patients. We are building an exceptional multi-disciplinary team with diverse expertise spanning healthcare, engineering, technology and regulatory, and with people who share our core value of Empowering Community through generosity, curiosity and humility. We are working with urgency to bring better therapies to patients faster.

Role Objectives and Responsibilities

• Own the vision, strategy, roadmap and requirements for the oncology data platform,aligned with N-Power's business goals and the needs of our ProECA studies.
• Manage the platform as a product: define its customers (biostatisticians, quantitativescientists, clinical operations, and pharma sponsors), set success metrics, and trackadoption and value.
• Collaborate with a cross-functional team of engineers, data architects, informaticists, AIengineers, quantitative scientists, clinical abstractors, and medical oncologists.
• Build regulatory-grade evidence into the platform: source-to-dataset traceability acrossEHR and imaging, data provenance, audit trails, and fit-for-purpose data quality alignedwith FDA guidance on external controls.
• Catalog and be able to point to end-user documentation for each data platform release:data dictionaries, vocabularies, CDISC-aligned specifications, data quality scorecards,licensing, and de-identification certifications.
• Produce external-facing collateral for pharma and health system partners: capabilitydecks, platform architecture, marketecture, data flow diagrams, and the data roadmap.
• Prioritize relentlessly and manage trade-offs across various data use cases.
• Manage releases, build vs. buy decisions, and the impact of platform changes on activestudies.
• Close process gaps in execution, rollout, and ongoing support through continuousstakeholder feedback.

Education, Experience, Behavioral Competencies, & Skills

• 8+ years of product management experience owning a healthcare data product in aregulated environment.
• Deep background in oncology clinical data: AJCC staging, histology, biomarker andgenomic testing, lines of therapy, RECIST-based response, progression, and survivalendpoints.
• Working command of FDA guidance on externally controlled trials, use of EHR data inclinical investigations, 21 CFR Part 11, ICH GCP, CDISC (SDTM, ADaM), and HIPAA.
• Deep knowledge of EHR data structures and workflows (HL7, FHIR), clinicalterminologies (ICD-10, SNOMED CT, LOINC, RxNorm, NCI Thesaurus), and datagovernance.
• Strong grounding in data platform architecture, data modeling, normalization, andtransformation.
• Experience writing functional and technical specifications for data platforms.
• Strong analytical skills and data intuition: uses metrics to evaluate decisions and driveaction.
• Exceptional written and verbal communication, with a track record of aligningoncologists, abstractors, biostatisticians, and engineers.
• Deep empathy for platform users, including quantitative scientists, epidemiologists, andstudy teams, and the ability to turn their needs into product requirements.

Preferred:

• Understanding of the oncology drug development lifecycle and how sponsors analyzedata across clinical development, regulatory, and medical affairs.
• Experience with prospective clinical research operations: protocols, EDC, source dataverification, monitoring, and inspection readiness.
• Experience with AI-assisted clinical data abstraction.
• Experience with data delivery and access platforms such as Databricks, Snowflake, andAPIs.
• Agile delivery with tools such as JIRA.

Travel Requirements

Up to 25% travel

Pay Information

The expected salary range for this position is $167,777 - $215,304. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. N-Power Medicine (NPM) offers equity at hire as well as a discretionary annual bonus, which may be available based on Company performance. This position is eligible for company benefits.

About Us:

We are a mission-driven, well-funded, rapidly growing company, eager to attract passionate professionals offering a highly attractive compensation package with a balanced and flexible work environment, competitive industry benefits as well as a 401K plan and other great company perks.

We are an Equal Opportunity Employer and value diversity at our company. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Applicants must be currently authorized